KIEHLS SINCE 1851 BLUE HERBAL ACNE SPOT TREATMENT- salicylic acid lotion

Kiehls Since 1851 Blue Herbal Acne Spot Treatment by

Drug Labeling and Warnings

Kiehls Since 1851 Blue Herbal Acne Spot Treatment by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc, L'Oreal USA, Inc., Cosmetic Essence, LLC dba Voyant Beauty, Paklab. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 2%

Purpose

Acne treatment

Use

for the treatment of acne

Warnings

For external use only

When using this product

skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. 

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• clean the skin thoroughly before applying this product
• cover the entire affected area with a thin layer one to three times daily
• because excessive drying of the skin may occur, start with one application daily, then gradually ingrease to two or three times dialy if neded or as directed by a doctor
• if bothersome dryness or peeling occurs, reduce application to once a day or every other dayl

Inactive ingredients

water, alcohol denat., glycerin, butylene glycol, methyl methacrylate crosspolymer, ammonium polyacryloyldimethyl taurate, perlite, nylon-12, dipropylene glycol, xanthan gum, peumus boldus leaf extract, boswellia serrata extract, hamamelis virginiana (witch hazel) water, t-butyl alcohol, camphor, menthol, zingiber officinale (ginger) root extract, sanguisorba officinalis root extract, cinnamomum cassia bark extract, phenoxyethanol, cinnamal, laminaria accharina extract, zinc sulfate, pyridoxine HCL, sodium hydroxide, citric acid

Questions or comments?

Call toll-free 1-800-946-4453

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KIEHLS SINCE 1851 BLUE HERBAL ACNE SPOT TREATMENT 
salicylic acid lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-527
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371)
PERLITE (UNII: 0SG101ZGK9)
NYLON-12 (UNII: 446U8J075B)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
XANTHAN GUM (UNII: TTV12P4NEE)
PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
MENTHOL (UNII: L7T10EIP3A)
GINGER (UNII: C5529G5JPQ)
SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X)
CHINESE CINNAMON (UNII: WS4CQ062KM)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CINNAMALDEHYDE (UNII: SR60A3XG0F)
SACCHARINA LATISSIMA (UNII: 68CMP2MB55)
ZINC SULFATE (UNII: 89DS0H96TB)
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-527-01	1 in 1 CARTON	08/31/2016	02/07/2025
1		15 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 49967-527-02	1.5 mL in 1 PACKET; Type 0: Not a Combination Product	08/31/2016	02/07/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	08/31/2016	02/07/2025

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
L'Oreal USA, Inc.		185931458	analysis(49967-527)

Establishment
Name	Address	ID/FEI	Business Operations
Cosmetic Essence, LLC dba Voyant Beauty		032565959	manufacture(49967-527)

Establishment
Name	Address	ID/FEI	Business Operations
Paklab		078717086	pack(49967-527)